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Disease association ontology term - MONDO:0003689 - familial hemolytic anemia

Term summary

ID
MONDO:0003689
Name
familial hemolytic anemia
Ontology or CV name
Disease association
Definition
A congenital hemolytic anemia caused by defects of the erythrocyte membrane, enzyme deficiencies, or hemoglobinopathies.

Parents

Annotation

Disease association

MONDO:0010480 - anemia, nonspherocytic hemolytic, due to G6PD deficiency

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MONDO:0009134 - congenital dyserythropoietic anemia type 2

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MONDO:0007109 - congenital dyserythropoietic anemia type 3

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MONDO:0006506 - congenital nonspherocytic hemolytic anemia

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MONDO:0008494 - cryohydrocytosis

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MONDO:0009902 - cutaneous porphyria

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MONDO:0012204 - familial pseudohyperkalemia

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MONDO:0009259 - gamma-glutamylcysteine synthetase deficiency

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MONDO:0009284 - glutathione synthetase deficiency without 5-oxoprolinuria

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MONDO:0009295 - glycogen storage disease VII

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MONDO:0009113 - hemolytic anemia due to diphosphoglycerate mutase deficiency

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MONDO:0013275 - hemolytic anemia due to glucophosphate isomerase deficiency

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MONDO:0019531 - hemolytic anemia due to glutathione reductase deficiency

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MONDO:0859172 - hemolytic disease of fetus and newborn, RH-induced

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MONDO:0012981 - hereditary spherocytosis type 4

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MONDO:0009340 - non-spherocytic hemolytic anemia due to hexokinase deficiency

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MONDO:0008493 - overhydrated hereditary stomatocytosis

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MONDO:0012992 - pancreatic insufficiency-anemia-hyperostosis syndrome

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MONDO:0009950 - pyruvate kinase deficiency of red cells

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MONDO:0012700 - renal tubular acidosis, distal, 4, with hemolytic anemia

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MONDO:0019107 - Rh deficiency syndrome

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MONDO:0008165 - southeast Asian ovalocytosis

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MONDO:0014221 - triosephosphate isomerase deficiency

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